ORPHA:596426
Syndrome of reduced sensitivity to thyroid hormone
- Type
- Clinical group
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Syndrome of reduced sensitivity to thyroid hormone | |
| fr | Syndrome de sensibilité réduite aux hormones thyroïdiennes | |
| de | Syndrome mit reduzierter Sensitivität gegenüber Schilddrüsenhormon | |
| es | Síndromes de sensibilidad reducida a las hormonas tiroideas | |
| it | Sindromi da ridotta sensibilità agli ormoni tiroidei | RTH |
| nl | Syndromen van gereduceerde gevoeligheid voor schildklierhormoon | RTH |
| pt | Síndromes de sensibilidade reduzida à hormona tiroideia | RTH |
| pl | Zespoły z obniżoną wrażliwością na hormony tarczycy | |
| cs | Syndrom snížené citlivosti na hormony štítné žlázy | |
| uk | Синдром зниженої чутливості до гормонів щитовидної залози | |
| zh | Syndrome of reduced sensitivity to thyroid hormone | |
| tr | Syndrome of reduced sensitivity to thyroid hormone |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C4722330 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:183631Rare genetic thyroid disease
rare genetic diseases - ORPHA:101955Rare thyroid disease
rare endocrine diseases
Children (5):
- ORPHA:59Allan-Herndon-Dudley syndrome
- ORPHA:597939Euthyroid dysprealbuminemic hyperthyroxinemia
- ORPHA:566231Resistance to thyroid hormone due to a mutation in thyroid hormone receptor alpha
- ORPHA:566243Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta
- ORPHA:171706Short stature-delayed bone age due to thyroid hormone metabolism deficiency
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/596426
- This record as JSON: /data/d/596426.json